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Omt Llc

FDA UDI

Class II (US FDA UDI)

by Omt, Llc

Identity

Trade Name
OMT LLC FDA UDI
Generic Name
Surgical/emergency suction cannula, non-illuminating, single-use FDA UDI
Device Name
Atraumatic-Malleable Disposable Suction; Sterile; 9 French [W]; 190mm [L] FDA UDI
Model / Reference
Round Tip FDA UDI
Description
Atraumatic-Malleable Disposable Suction; Sterile; 9 French [W]; 190mm [L] FDA UDI

Identifiers

Catalog Number
RT-0990 FDA UDI
Primary DI / UDI-DI
M731RT09900 FDA UDI
FDA Product Code
GCX FDA UDI
GMDN Term
Surgical/emergency suction cannula, non-illuminating, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical/emergency suction cannula, non-illuminating, single-use

Omt Llc by Omt, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical/emergency suction cannula, non-illuminating, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Omt, Llc

Sources (1)

  • FDA UDI da187736-620c-4515-a775-de7206a8bcb5 35 fields · synced Jun 8, 2026